TY - JOUR
T1 - Annihilation of structural defects in chalcogenide absorber films for high-efficiency solar cells
AU - Mainz, Roland
AU - Simsek Sanli, Ekin
AU - Stange, Helena
AU - Azulay, Doron
AU - Brunken, Stephan
AU - Greiner, Dieter
AU - Hajaj, Shir
AU - Heinemann, Marc D.
AU - Kaufmann, Christian A.
AU - Klaus, Manuela
AU - Ramasse, Quentin M.
AU - Rodriguez-Alvarez, Humberto
AU - Weber, Alfons
AU - Balberg, Isaac
AU - Millo, Oded
AU - Van Aken, Peter A.
AU - Abou-Ras, Daniel
N1 - Funding Information: The work was partly funded by the Helmholtz Virtual Institute HVI-520 Microstructure Control for Thin-Film Solar Cells, and by the European Metrology Research Programme (EMRP) Project IND07 Thin Films and Project ThinErgy. The EMRP is jointly funded by the EMRP participating countries within EURAMET and the European Union. SuperSTEM is the U.K. National Facility for Aberration-Corrected STEM, supported by the Engineering and Physical Sciences Research Council (EPSRC). Publisher Copyright: © 2016 The Royal Society of Chemistry.
PY - 2016/5
Y1 - 2016/5
N2 - In polycrystalline semiconductor absorbers for thin-film solar cells, structural defects may enhance electron-hole recombination and hence lower the resulting energy conversion efficiency. To be able to efficiently design and optimize fabrication processes that result in high-quality materials, knowledge of the nature of structural defects as well as their formation and annihilation during film growth is essential. Here we show that in co-evaporated Cu(In,Ga)Se2 absorber films the density of defects is strongly influenced by the reaction path and substrate temperature during film growth. A combination of high-resolution electron microscopy, atomic force microscopy, scanning tunneling microscopy, and X-ray diffraction shows that Cu(In,Ga)Se2 absorber films deposited at low temperature without a Cu-rich stage suffer from a high density of-partially electronically active-planar defects in the {112} planes. Real-time X-ray diffraction reveals that these faults are nearly completely annihilated during an intermediate Cu-rich process stage with [Cu]/([In] + [Ga]) > 1. Moreover, correlations between real-time diffraction and fluorescence analysis during Cu-Se deposition reveal that rapid defect annihilation starts shortly before the start of segregation of excess Cu-Se at the surface of the Cu(In,Ga)Se2 film. The presented results hence provide direct insights into the dynamics of the film-quality-improving mechanism.
AB - In polycrystalline semiconductor absorbers for thin-film solar cells, structural defects may enhance electron-hole recombination and hence lower the resulting energy conversion efficiency. To be able to efficiently design and optimize fabrication processes that result in high-quality materials, knowledge of the nature of structural defects as well as their formation and annihilation during film growth is essential. Here we show that in co-evaporated Cu(In,Ga)Se2 absorber films the density of defects is strongly influenced by the reaction path and substrate temperature during film growth. A combination of high-resolution electron microscopy, atomic force microscopy, scanning tunneling microscopy, and X-ray diffraction shows that Cu(In,Ga)Se2 absorber films deposited at low temperature without a Cu-rich stage suffer from a high density of-partially electronically active-planar defects in the {112} planes. Real-time X-ray diffraction reveals that these faults are nearly completely annihilated during an intermediate Cu-rich process stage with [Cu]/([In] + [Ga]) > 1. Moreover, correlations between real-time diffraction and fluorescence analysis during Cu-Se deposition reveal that rapid defect annihilation starts shortly before the start of segregation of excess Cu-Se at the surface of the Cu(In,Ga)Se2 film. The presented results hence provide direct insights into the dynamics of the film-quality-improving mechanism.
UR - http://www.scopus.com/inward/record.url?scp=84970974296&partnerID=8YFLogxK
U2 - https://doi.org/10.1039/c6ee00402d
DO - https://doi.org/10.1039/c6ee00402d
M3 - Article
SN - 1754-5692
VL - 9
SP - 1818
EP - 1827
JO - Energy and Environmental Science
JF - Energy and Environmental Science
IS - 5
ER -